| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs578248951 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | INTS12 | GRCh38.p7 | 4:105684223 | CTCTTGTTCACACAA[G/T]AATATATTTTTTCAC | 57117 |
| rs745340063 | in-del | -/ACTGGTCTCCTCAAA | 1.64783e-05 | 0.00287034 | cds-indel, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105693346 | GGCAAAATCATCAGC[-/ACTGGTCTCCTCAAA]ACTGGAAAGGTCAGC | 57117 |
| rs745420681 | snp | A/G | 6.59207e-05 | 0.00574073 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105683188 | TGTTTTGTGTTGTTG[A/G]ACTCAATTTTGCTGT | 57117 |
| rs745435204 | in-del | -/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105697901 | CAAAATATAAAAAAA[-/T]TAGCCAAGCATGGTG | 57117 |
| rs745439892 | snp | A/C | | | intron-variant | INTS12 | GRCh38.p7 | 4:105683675 | GTTAAACATCTAATT[A/C]TTTTAGACTTTTCTC | 57117 |
| rs745458276 | snp | G/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105696656 | ACTATTACAAATAAA[G/T]CTGTTATGAATATTC | 57117 |
| rs745814045 | snp | A/C | 1.92125e-05 | 0.00309933 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105692017 | GGGCACAATACCACA[A/C]CAGGCGAGGGTCATT | 57117 |
| rs745937062 | snp | C/T | 1.68624e-05 | 0.0029036 | intron-variant | INTS12 | GRCh38.p7 | 4:105686886 | AATCTTAACTGAATA[C/T]ACAGAAAGATAATAA | 57117 |
| rs745955832 | in-del | -/T | | | upstream-variant-2KB, intron-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105710387 | ATCACACTCGGCTCC[-/T]TTTTTTTTTTTTTTT | 57117 |
| rs746020810 | snp | G/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | INTS12, GSTCD | GRCh38.p7 | 4:105708254 | GAATGTCAATCCTTT[G/T]ATCAAAGCATCACAC | 57117 |
| rs746202124 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105698933 | AGTGATTTGGAGTTT[A/G]AGGGTCAGAGCTTAG | 57117 |
| rs746272951 | snp | C/T | | | intron-variant, upstream-variant-2KB | INTS12, GSTCD | GRCh38.p7 | 4:105707145 | GTCCAGGAAGCTCTT[C/T]ACCTATTTTTATATA | 57117 |
| rs746311281 | in-del | -/T | | | intron-variant, upstream-variant-2KB | INTS12, GSTCD | GRCh38.p7 | 4:105707681 | TTTCGCCTGTCTTGC[-/T]TAATTCATTAATCCC | 57117 |
| rs746414355 | snp | A/G | 1.67105e-05 | 0.0028905 | intron-variant | INTS12 | GRCh38.p7 | 4:105693517 | ATCAGAAAATGATAA[A/G]GTAATGTGGTAGAAT | 57117 |
| rs746483049 | in-del | -/GAAGA | | | intron-variant | INTS12 | GRCh38.p7 | 4:105690078 | AACAGTATCCCAGAT[-/GAAGA]GAAGAAGCTGAGAAG | 57117 |
| rs746618986 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105701944 | AGATTACAAGACTGC[A/G]GAAGTCATCAACACC | 57117 |
| rs746706649 | in-del | -/TT | | | intron-variant | INTS12 | GRCh38.p7 | 4:105701235 | ACACATCCCTAGGCT[-/TT]TTTTTTTTTTTTTTT | 57117 |
| rs746873017 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105706666 | CCGAAAAGTTCCTTG[C/T]CCTGCTCTTACTTTC | 57117 |
| rs746924226 | snp | A/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105694232 | CTAAAAGAAATCTAG[A/T]TCTACATGCATTAAC | 57117 |
| rs747052877 | snp | C/T | 1.72065e-05 | 0.00293308 | intron-variant | INTS12 | GRCh38.p7 | 4:105693258 | AGGGTCATGTGTTCT[C/T]TATAAAGTAACAAAA | 57117 |
| rs747084855 | snp | A/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105700430 | CAAGGGAAGACTTAG[A/T]GTGCAGGTGTTTGTG | 57117 |
| rs747158726 | snp | G/T | 1.88042e-05 | 0.00306623 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105692042 | GTCATTCGCTTCCTT[G/T]TCTGTCACCTGGGGT | 57117 |
| rs747436649 | snp | G/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105695212 | TCTATCTTTTCTTCT[G/T]AACAACTGTTCCATC | 57117 |
| rs747465112 | snp | A/G | 1.64735e-05 | 0.00286993 | synonymous-codon, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105683044 | GTGGAGGTGGTTTTA[A/G]AGGTACAGTGGGCGT | 57117 |
| rs747473268 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105689283 | CAGTTTGAGGAATCT[A/G]TTTGAGGAGAAAGGG | 57117 |
| rs747647150 | snp | G/T | 1.64784e-05 | 0.00287035 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105695578 | TGAGGACCTTGCCAT[G/T]ATTATTACCAGAAGG | 57117 |
| rs747732436 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105705079 | AATTCTCTACATCAG[A/G]GGTCCCTAACCTTCA | 57117 |
| rs747736204 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105694412 | CTCACTGTAACCTCC[A/G]CCTGCTGGGTTAGAG | 57117 |
| rs747785227 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105696514 | TATTTTGAGATTCAT[C/T]CATGTTGTTTAGTGT | 57117 |
| rs747969661 | snp | A/C | 1.70927e-05 | 0.00292336 | intron-variant | INTS12 | GRCh38.p7 | 4:105686680 | CTTAGATAAAAATAG[A/C]ATCTACTATACCTTG | 57117 |
| rs747972714 | in-del | CACCCTTTTGGCCCG/TCACCATGTT | | | upstream-variant-2KB, intron-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105710424 | AGTCGAGGAGGGGTT[CACCCTTTTGGCCCG/TCACCATGTT]GGCCAGGCTGGTCTC | 57117 |
| rs748031267 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105695003 | GATCACCGCTCACTG[C/T]AATCTCTGCCTCCTG | 57117 |
| rs748144462 | snp | A/G/T | 8.23616e-05 | 0.00641679 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | INTS12, ARHGEF38 | GRCh38.p7 | 4:105682814 | CTGTGATTCTTGTGA[A/G/T]GTTGGGCCTTTAAGG | 57117 |
| rs748223725 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105689638 | CCTGGCATGGTGGCT[C/T]ATGCCTATAATCCCA | 57117 |
| rs748225262 | snp | G/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105702622 | ACAATCTTCCATTAC[G/T]CTATCTCTTCCACTG | 57117 |
| rs748276814 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105691044 | TACTACTTTTTATTT[C/T]ATAGGAATAAATAAA | 57117 |
| rs748332752 | snp | A/T | 1.64866e-05 | 0.00287106 | synonymous-codon, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105693463 | CTTTGGAATATCAAC[A/T]CCTTCAGTGATGTCT | 57117 |
| rs748384283 | snp | G/T | 1.70295e-05 | 0.00291796 | intron-variant | INTS12 | GRCh38.p7 | 4:105693274 | TATAAAGTAACAAAA[G/T]AATCTGTGGCAAGGT | 57117 |
| rs748564001 | snp | A/C | | | intron-variant | INTS12 | GRCh38.p7 | 4:105697991 | GGAGGGAGAGAGCGC[A/C]GTGAGCCAAGATTGT | 57117 |
| rs748659163 | snp | C/T | 1.6476e-05 | 0.00287014 | synonymous-codon, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105683165 | CGAAGTAGCAGGTTT[C/T]CCAGTATTGTTTTGT | 57117 |
| rs748674365 | in-del | -/T | 3.29495e-05 | 0.00405877 | frameshift-variant, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105693445 | TTTCTCCAATCTAGG[-/T]TTCTTTGGAATATCA | 57117 |
| rs748791802 | snp | A/G | 9.88484e-05 | 0.00702954 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105683058 | AAAGGTACAGTGGGC[A/G]TAGTGCTGTTATTGG | 57117 |
| rs748798493 | snp | C/T | 1.75105e-05 | 0.00295888 | intron-variant | INTS12 | GRCh38.p7 | 4:105699843 | AGCTTTTTATTCATT[C/T]AAGTACCTTTTGAGA | 57117 |
| rs748817948 | snp | C/T | 1.6888e-05 | 0.00290581 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105699999 | CCAAGTTCACAGTAG[C/T]AGCCATTGCAAACGC | 57117 |
| rs748831033 | snp | C/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | INTS12, GSTCD | GRCh38.p7 | 4:105708262 | ATCCTTTGATCAAAG[C/G]ATCACACATCGAAGT | 57117 |
| rs749033718 | snp | C/T | 2.07127e-05 | 0.00321806 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105691996 | TTTTCATTTGTCTGG[C/T]ACATCGGGCACAATA | 57117 |
| rs749084126 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105703125 | CATGGCCAAAACAGA[C/T]TGCAAAAGAGCCATA | 57117 |
| rs749175970 | in-del | -/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105683327 | GGATGTCTAAAAAAA[-/T]AAAGTAAATAATTAC | 57117 |
| rs749476434 | snp | A/G | 1.64743e-05 | 0.00287 | missense, nc-transcript-variant, downstream-variant-500B | INTS12, ARHGEF38 | GRCh38.p7 | 4:105682944 | CTGCTTCCTGGAACT[A/G]AACTACTTGGACTAG | 57117 |
| rs749480000 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105692393 | GGAGGCTGAGGCAGG[A/G]GAATCGCTTGAACCC | 57117 |
| rs749481808 | snp | G/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105691213 | ATGAGAACTCTGCAA[G/T]TGAGAATCACTAATT | 57117 |
| rs749527653 | snp | G/T | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant, downstream-variant-500B | INTS12, ARHGEF38 | GRCh38.p7 | 4:105682830 | GTTGGGCCTTTAAGG[G/T]ATGCTGAGGGAGAGC | 57117 |
| rs749655476 | snp | C/T | 1.65007e-05 | 0.00287229 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105693474 | CAACTCCTTCAGTGA[C/T]GTCTGATTTCATCTA | 57117 |
| rs749662473 | snp | G/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105699093 | CAACTCTGCAAAGTA[G/T]TTCTTATTATCCCCA | 57117 |
| rs749665785 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105684000 | ATTTGCCCATGATTC[C/T]GGTTAAACTATCATG | 57117 |
| rs749701049 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105698167 | TGTTCTAGTTGTTGA[C/T]GGATGAGTTAAGTTT | 57117 |
| rs749722938 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105685618 | TTAGATAAGGCAATA[A/G]CTTTAGAGTTTTCTC | 57117 |
| rs749724179 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105702358 | AGCCAGGATGGTCTC[A/G]ATCTCCTGACCTTGT | 57117 |
| rs749959276 | snp | C/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105698750 | CAATAAAAAGGCTTC[C/G]GAGTACTAGACCTAG | 57117 |
| rs749960712 | snp | C/G | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105708905 | GTCTGCGGGCAGCAG[C/G]TCCCAGAGGCAGCCT | 57117 |
| rs750008057 | snp | A/G | 4.94344e-05 | 0.00497139 | missense, nc-transcript-variant, downstream-variant-500B | INTS12, ARHGEF38 | GRCh38.p7 | 4:105682888 | TAGTACTTCCACTAG[A/G]TCCTGATGTTCCACT | 57117 |
| rs750131305 | snp | C/T | 1.64754e-05 | 0.00287009 | missense, nc-transcript-variant, downstream-variant-500B | INTS12, ARHGEF38 | GRCh38.p7 | 4:105682782 | TTGACCATCTGTAAT[C/T]GCTTCATAGCATTGA | 57117 |
| rs750184338 | snp | A/T | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105693377 | CTGGAAAGGTCAGCC[A/T]TAGGTAAATCCTTGC | 57117 |
| rs750283548 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105706552 | AAATCTCTTAAATTT[A/G]AATCCCATGTTTCCA | 57117 |
| rs750315329 | snp | C/T | 2.37054e-05 | 0.00344269 | intron-variant | INTS12 | GRCh38.p7 | 4:105692170 | AACATTACACTACTT[C/T]TTTAAATGCCATAAT | 57117 |
| rs750492849 | snp | A/G | 1.65759e-05 | 0.00287883 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105683250 | AAAGCTGCCCATCCA[A/G]TTAAGCCACTAGTTA | 57117 |
| rs750507123 | in-del | -/TTT | | | intron-variant | INTS12 | GRCh38.p7 | 4:105701234 | TACACATCCCTAGGC[-/TTT]TTTTTTTTTTTTTTT | 57117 |
| rs750573513 | snp | C/T | | | intron-variant, upstream-variant-2KB | INTS12, GSTCD | GRCh38.p7 | 4:105707555 | AAAGTAACTCACCCC[C/T]GCCCCCACAAAAAAA | 57117 |
| rs750621636 | snp | A/G | 1.75342e-05 | 0.00296087 | intron-variant | INTS12 | GRCh38.p7 | 4:105700033 | AAGGAAAAAAAGAGA[A/G]AGTAATCTAGAAGAC | 57117 |
| rs750626899 | snp | C/T | 9.9346e-05 | 0.00704721 | synonymous-codon, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105699958 | ATGCAAGAAACCTAG[C/T]GCTTTCAAAAAAATG | 57117 |
| rs750630416 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105694162 | ATGATAAACTGGTTA[A/G]TCATTCCCCTATGAT | 57117 |
| rs750685563 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105694776 | TCAAATGTATTTTTT[C/T]CTAACTACTAAAATC | 57117 |
| rs750799254 | snp | C/T | 3.57667e-05 | 0.00422872 | intron-variant | INTS12 | GRCh38.p7 | 4:105699812 | TAGTACTACAGGCCT[C/T]ACAAAACTCTCTCCA | 57117 |
| rs750828501 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105688544 | TGTTCGAAGTAATTC[A/G]CTGTTGATTACTTGA | 57117 |
| rs750922937 | in-del | -/TTTAA | | | intron-variant | INTS12 | GRCh38.p7 | 4:105685265 | AATATGACAGCAGTC[-/TTTAA]TTTGTTTGCCATAAA | 57117 |
| rs751058831 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105706420 | CCACCGTAACCATGC[C/T]CAGGTAATTTTGTTG | 57117 |
| rs751076814 | snp | C/G | | | intron-variant, utr-variant-5-prime, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105703660 | TACATTCTATCTTCA[C/G]AATCACCATTCTCAG | 57117 |
| rs751080508 | snp | A/G | 1.66252e-05 | 0.00288311 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105686837 | TTCTGAGTTTTTTGA[A/G]CCTGCAAAAATCAGT | 57117 |
| rs751209276 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105698990 | GTATTAGGGAATATA[A/G]TAAGAGTTGTCATTC | 57117 |
| rs751262791 | snp | A/G | | | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105699947 | TTACTCTTTGAATGC[A/G]AGAAACCTAGTGCTT | 57117 |
| rs751290413 | snp | A/G | 4.94222e-05 | 0.00497078 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | INTS12, ARHGEF38 | GRCh38.p7 | 4:105682910 | TGTTCCACTATTTCC[A/G]TTCCCACTTAGTTGG | 57117 |
| rs751359943 | snp | A/G | | | upstream-variant-2KB | INTS12, GSTCD | GRCh38.p7 | 4:105708764 | GGGAAACGTTTGGCA[A/G]TGCGACAGTAGGAAG | 57117 |
| rs751365678 | snp | C/G | | | intron-variant, upstream-variant-2KB | INTS12, GSTCD | GRCh38.p7 | 4:105707813 | CGAACTAGGTTTTTT[C/G]CGTAAATGTCACCTT | 57117 |
| rs751420784 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105694921 | CTTTCCCATCTTTTC[C/T]TTCTTGCTTTCCTTT | 57117 |
| rs751457421 | snp | C/T | 1.64754e-05 | 0.00287009 | missense, nc-transcript-variant, downstream-variant-500B | INTS12, ARHGEF38 | GRCh38.p7 | 4:105682789 | TCTGTAATCGCTTCA[C/T]AGCATTGAGCTGTGA | 57117 |
| rs751527108 | snp | C/G/T | 3.29474e-05 | 0.00405867 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105693440 | TCTGGTTTCTCCAAT[C/G/T]TAGGTTTCTTTGGAA | 57117 |
| rs751741635 | snp | A/C | 2.13149e-05 | 0.00326451 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105683307 | GAATTTCCTGAAATA[A/C]CTGTGGATGTCTAAA | 57117 |
| rs751836037 | snp | A/G | 3.3243e-05 | 0.00407681 | synonymous-codon, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105683258 | CCATCCAGTTAAGCC[A/G]CTAGTTACTGACGAG | 57117 |
| rs751890939 | snp | A/C | 3.5727e-05 | 0.00422637 | intron-variant | INTS12 | GRCh38.p7 | 4:105700048 | AAGTAATCTAGAAGA[A/C]AATGCACAATTATCT | 57117 |
| rs752014278 | snp | C/T | 1.6571e-05 | 0.0028784 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105699962 | AAGAAACCTAGTGCT[C/T]TCAAAAAAATGGGAT | 57117 |
| rs752020583 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105703497 | TTCCTATCCAGCTCA[C/T]ATTCTGTGGTCCACC | 57117 |
| rs752073430 | snp | C/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105690842 | AATTTCCAATTCTTA[C/G]TGGTTTCTTATCAAT | 57117 |
| rs752345091 | snp | C/T | 2.47565e-05 | 0.00351818 | splice-donor-variant | INTS12 | GRCh38.p7 | 4:105691975 | AAAATATGATTCCTA[C/T]CATTCTTTTCATTTG | 57117 |
| rs752359029 | snp | C/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105701625 | CATATACAAGGGTAA[C/G]AGCCTAATCTCTTTT | 57117 |
| rs752415126 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105688794 | CCCAGGAAGTACTTC[C/T]GCCTGTGAGATCATG | 57117 |
| rs752441995 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105687681 | GGGTGCAGTGGCTCA[C/T]GCCTGTAATCCCAGC | 57117 |
| rs752500587 | in-del | -/A | | | intron-variant | INTS12 | GRCh38.p7 | 4:105685244 | CAAAACCTCTTAATC[-/A]AAACAAATATGACAG | 57117 |
| rs752538633 | snp | A/C | 3.29457e-05 | 0.00405854 | missense, nc-transcript-variant, downstream-variant-500B | INTS12, ARHGEF38 | GRCh38.p7 | 4:105683017 | TAAGGCCAGTTTTAC[A/C]CAAGGTTAGAGGTGG | 57117 |
| rs752551547 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105697269 | GCTCTTGGAATTCCC[C/T]CTCCCCCAAAAGGAG | 57117 |
| rs752578495 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105708839 | GCCGGCGCGAGTATT[C/T]TCCACATAAGGTGGC | 57117 |
| rs752598398 | snp | A/G | | | intron-variant, downstream-variant-500B, nc-transcript-variant | INTS12, ARHGEF38 | GRCh38.p7 | 4:105682368 | AAACTATGTTGGGTC[A/G]TCCCTGCCGCCACAT | 57117 |
| rs752693396 | snp | A/G | 3.32094e-05 | 0.00407475 | intron-variant | INTS12 | GRCh38.p7 | 4:105695681 | ATCCTAAAAGATGAA[A/G]AAAGGTACCAGTAAT | 57117 |
| rs752694247 | snp | A/G | 1.6473e-05 | 0.00286988 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | INTS12, ARHGEF38 | GRCh38.p7 | 4:105682928 | CCCACTTAGTTGGCT[A/G]CTGCTTCCTGGAACT | 57117 |
| rs752716372 | snp | A/C | | | intron-variant | INTS12 | GRCh38.p7 | 4:105703629 | AAACTCTAAGTGCAA[A/C]TGGGAGGAATATACA | 57117 |
| rs752762393 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105694003 | CAATGCCTAGTAATG[C/T]TGAAGATGTCATATC | 57117 |
| rs752990079 | snp | A/T | | | upstream-variant-2KB, intron-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105709958 | TAATAAACATTAAGC[A/T]ATGCGGGTTTTTTTT | 57117 |
| rs753030265 | snp | A/C | 2.85059e-05 | 0.0037752 | intron-variant | INTS12 | GRCh38.p7 | 4:105683321 | AACTGTGGATGTCTA[A/C]AAAAATAAAGTAAAT | 57117 |
| rs753268208 | snp | A/G | 1.65056e-05 | 0.00287272 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | INTS12, ARHGEF38 | GRCh38.p7 | 4:105682742 | GCCACATTACTTCTT[A/G]AGTTTCTTTTGGGCA | 57117 |
| rs753403743 | snp | C/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105684333 | TCTTAAGAAGATTCA[C/G]AAAAGCATTACATTC | 57117 |
| rs753451815 | snp | C/T | 1.64781e-05 | 0.00287033 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105693342 | CCATGGCAAAATCAT[C/T]AGCACTGGTCTCCTC | 57117 |
| rs753497687 | snp | A/C | | | intron-variant | INTS12 | GRCh38.p7 | 4:105690618 | AAGTATCTATAGACT[A/C]TCTAGTTAGCTATAG | 57117 |
| rs753731179 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105697682 | TACTATTTGGCTCTT[C/T]ATAAAGTCTGTTGAT | 57117 |
| rs753757866 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105688139 | AGTGTCTGGAAAATG[C/T]TGAGTGCTAACAAAA | 57117 |
| rs753783470 | snp | A/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105683615 | CTGAAAACCAGATTT[A/T]GTGCTTTAACATAGT | 57117 |
| rs753784829 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105698489 | GGGCAGCGTGCTTTT[C/T]AATCACAACAAATTT | 57117 |
| rs753888147 | snp | C/T | 1.6476e-05 | 0.00287014 | synonymous-codon, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105683114 | TTTGGATGATGTTGC[C/T]AGACCAGTCAAACCC | 57117 |
| rs753919593 | snp | A/G | 1.65203e-05 | 0.002874 | synonymous-codon, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105699915 | CAAGCAGTGCTTTTA[A/G]CTTTTCAGCAGAATC | 57117 |
| rs753942504 | snp | A/G | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant, downstream-variant-500B | INTS12, ARHGEF38 | GRCh38.p7 | 4:105683028 | TTACCCAAGGTTAGA[A/G]GTGGAGGTGGTTTTA | 57117 |
| rs753955357 | snp | C/T | 1.67022e-05 | 0.00288978 | intron-variant | INTS12 | GRCh38.p7 | 4:105695703 | ACCAGTAATTAAATA[C/T]TTAGACTGATCATCA | 57117 |
| rs754068846 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105704639 | ACTGCCAGCTTGACA[C/T]GGATATATCATTGGT | 57117 |
| rs754230359 | in-del | -/TAAGT | | | intron-variant | INTS12 | GRCh38.p7 | 4:105697061 | TGTTTGTTTTATTAC[-/TAAGT]TAAAAGAGTTCTTCA | 57117 |
| rs754317938 | snp | C/T | 7.2767e-05 | 0.00603143 | intron-variant | INTS12 | GRCh38.p7 | 4:105683342 | TAAAGTAAATAATTA[C/T]ATTAGAGCCAAGTTT | 57117 |
| rs754479657 | snp | A/C | 2.90905e-05 | 0.00381371 | intron-variant | INTS12 | GRCh38.p7 | 4:105691961 | GTTTAAAATAAAGAA[A/C]AATATGATTCCTACC | 57117 |
| rs754516738 | snp | G/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105687056 | AAGATAATATTAAGC[G/T]TTAGAAATAATACAG | 57117 |
| rs754600333 | snp | C/G | 1.66416e-05 | 0.00288453 | intron-variant | INTS12 | GRCh38.p7 | 4:105686842 | AGTTTTTTGAGCCTG[C/G]AAAAATCAGTGGATT | 57117 |
| rs754894170 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105698298 | ATTACCTCCAGGTGA[C/T]TCTTATCCATGCTAA | 57117 |
| rs754894181 | snp | C/G | 1.64738e-05 | 0.00286995 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | INTS12, ARHGEF38 | GRCh38.p7 | 4:105682796 | TCGCTTCATAGCATT[C/G]AGCTGTGATTCTTGT | 57117 |
| rs755133435 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105689701 | TGAGGTCAGGAGTTC[A/G]AGACCAGCCCTGGCA | 57117 |
| rs755161854 | snp | A/C | | | intron-variant, downstream-variant-500B, nc-transcript-variant | INTS12, ARHGEF38 | GRCh38.p7 | 4:105682185 | ATAAAAAAGGTAAAG[A/C]TATAATATGAAGTAT | 57117 |
| rs755268999 | snp | A/G | 1.66579e-05 | 0.00288595 | synonymous-codon, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105683261 | TCCAGTTAAGCCACT[A/G]GTTACTGACGAGGAA | 57117 |
| rs755313722 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105691637 | CTCAACAAAGAGTGG[A/G]GCTTTGTATCTCACC | 57117 |
| rs755393408 | snp | A/G | 1.79326e-05 | 0.00299432 | intron-variant | INTS12 | GRCh38.p7 | 4:105700050 | GTAATCTAGAAGACA[A/G]TGCACAATTATCTAT | 57117 |
| rs755401796 | snp | A/G | 3.29495e-05 | 0.00405877 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105683154 | TGGTTAGCTGACGAA[A/G]TAGCAGGTTTCCCAG | 57117 |
| rs755408831 | snp | A/G | | | upstream-variant-2KB, intron-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105710593 | CTGTGATTTTTAAAT[A/G]AAAATAAATACTGAG | 57117 |
| rs755548154 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105690862 | TTCTTATCAATGCTC[C/T]GGAATGCATTGCTCA | 57117 |
| rs755578840 | snp | C/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | INTS12, GSTCD | GRCh38.p7 | 4:105708022 | ATCGTTGCCATTTCA[C/T]AATGGCTCTAAAAAA | 57117 |
| rs755677278 | snp | C/T | | | intron-variant, downstream-variant-500B, nc-transcript-variant | INTS12, ARHGEF38 | GRCh38.p7 | 4:105682163 | CTTAAATAATTGAAA[C/T]GAGGTGATAAAAAAG | 57117 |
| rs755758231 | snp | C/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105689084 | AATAGGAGTGTGTTA[C/G]TACCTTAGATTGAGA | 57117 |
| rs755843749 | snp | C/T | | | intron-variant, downstream-variant-500B, nc-transcript-variant | INTS12, ARHGEF38 | GRCh38.p7 | 4:105682373 | ATGTTGGGTCGTCCC[C/T]GCCGCCACATAAGGC | 57117 |
| rs755845849 | in-del | -/C | 1.64732e-05 | 0.0028699 | frameshift-variant, nc-transcript-variant, downstream-variant-500B | INTS12, ARHGEF38 | GRCh38.p7 | 4:105682965 | CTTGGACTAGGAAGA[-/C]CTACTTTGCTGACAT | 57117 |
| rs755970575 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105683499 | TTATCATTTGCAAAG[C/T]AGAAAATTTTTGATA | 57117 |
| rs756115009 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105696320 | TATAGAAAAATATGT[C/T]TCCCATCATCAAGCA | 57117 |
| rs756118798 | snp | A/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105704550 | ATTATTGCCCTAGAC[A/T]ATTTGATCTATATAG | 57117 |
| rs756144174 | snp | C/T | 1.6473e-05 | 0.00286988 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | INTS12, ARHGEF38 | GRCh38.p7 | 4:105683018 | AAGGCCAGTTTTACC[C/T]AAGGTTAGAGGTGGA | 57117 |
| rs756173911 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105692258 | GGAGGCCAAGGCAGG[C/T]GGATCATTTGAAGTC | 57117 |
| rs756195030 | snp | C/T | 1.66524e-05 | 0.00288547 | intron-variant | INTS12 | GRCh38.p7 | 4:105695690 | GATGAAAAAAGGTAC[C/T]AGTAATTAAATATTT | 57117 |
| rs756199076 | snp | A/C/G | 3.29485e-05 | 0.00405874 | missense, nc-transcript-variant, downstream-variant-500B | INTS12, ARHGEF38 | GRCh38.p7 | 4:105682939 | GGCTGCTGCTTCCTG[A/C/G]AACTAAACTACTTGG | 57117 |
| rs756319736 | snp | A/T | 1.64904e-05 | 0.00287139 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105695540 | AGGTCTCTTTTCAGC[A/T]TCCTTCTTTACCTTT | 57117 |
| rs756346757 | in-del | -/TCT | | | intron-variant | INTS12 | GRCh38.p7 | 4:105703445 | TCTTTTTTCTGTATC[-/TCT]TATTATCCTTGATTT | 57117 |
| rs756357331 | in-del | -/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105695308 | TTTATTGACAATAAC[-/T]TTTAACCACTTAACT | 57117 |
| rs756504893 | snp | A/C | 3.6706e-05 | 0.00428388 | intron-variant | INTS12 | GRCh38.p7 | 4:105683325 | GTGGATGTCTAAAAA[A/C]ATAAAGTAAATAATT | 57117 |
| rs756508949 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105688843 | CCTGTTTTATCCAGC[C/T]ATCTTAGAAACTGAG | 57117 |
| rs756562917 | snp | A/C | | | intron-variant | INTS12 | GRCh38.p7 | 4:105699038 | TACCAGGCAGGTACT[A/C]CACTAGGTAACTCAT | 57117 |
| rs756686364 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105696558 | TCCTTTTTATTGCTG[A/G]ATAATATTCCATTGA | 57117 |
| rs756834645 | snp | C/T | 1.64923e-05 | 0.00287156 | missense, nc-transcript-variant, downstream-variant-500B | INTS12, ARHGEF38 | GRCh38.p7 | 4:105682749 | TACTTCTTGAGTTTC[C/T]TTTGGGCAGCTTTCT | 57117 |
| rs756845664 | in-del | -/TAAAG | 7.3377e-05 | 0.00605666 | intron-variant | INTS12 | GRCh38.p7 | 4:105683327 | GGATGTCTAAAAAAA[-/TAAAG]TAAATAATTACATTA | 57117 |
| rs756903334 | snp | A/G | | | intron-variant, utr-variant-5-prime, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105703682 | CATTCTCAGCTTGGC[A/G]TTCAGTACAACTTGG | 57117 |
| rs756921427 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105708956 | GGCGGGAAGGCGCAG[A/G]CGGCCCAGGTCGCCG | 57117 |
| rs757103902 | snp | A/G | 2.03564e-05 | 0.00319027 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105691999 | TCATTTGTCTGGTAC[A/G]TCGGGCACAATACCA | 57117 |
| rs757345049 | snp | A/C | 1.64749e-05 | 0.00287005 | synonymous-codon, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105683117 | GGATGATGTTGCCAG[A/C]CCAGTCAAACCCACA | 57117 |
| rs757385899 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105694065 | TAGAAACTATTAACA[C/T]GACATATGTATAAAG | 57117 |
| rs757399013 | in-del | -/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105686516 | CAACAGAGTTAGAGA[-/T]TAATTAATGATATAA | 57117 |
| rs757474937 | snp | A/G | 1.68021e-05 | 0.0028984 | intron-variant | INTS12 | GRCh38.p7 | 4:105695715 | ATATTTAGACTGATC[A/G]TCATAAAAAAAGATC | 57117 |
| rs757482103 | snp | A/G | 9.88338e-05 | 0.00702902 | missense, nc-transcript-variant, downstream-variant-500B | INTS12, ARHGEF38 | GRCh38.p7 | 4:105683029 | TACCCAAGGTTAGAG[A/G]TGGAGGTGGTTTTAA | 57117 |
| rs757516945 | in-del | -/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105706254 | CCCAACTTCAATCTC[-/T]TTTTTTTTTTTTTTT | 57117 |
| rs757563184 | snp | G/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105692399 | TGAGGCAGGAGAATC[G/T]CTTGAACCCAGGAGA | 57117 |
| rs757580917 | snp | A/C | | | intron-variant | INTS12 | GRCh38.p7 | 4:105701718 | GGTAAAGGAAATAGC[A/C]GTTTACTTATCCAGA | 57117 |
| rs757623512 | snp | C/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105706418 | CACCACCGTAACCAT[C/G]CCCAGGTAATTTTGT | 57117 |
| rs757721714 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105687632 | GTAATTTTCAGAGTC[A/G]AACACAGTTAGGATT | 57117 |
| rs757887880 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105701671 | ACTCCTGTGACAGTT[C/T]ACTAATCTTTCTACT | 57117 |
| rs757902634 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105698768 | GTACTAGACCTAGTA[C/T]TGAAAGAAGGCTGGG | 57117 |
| rs757955649 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105685198 | AAATTTATTCACTTT[C/T]ATAAAAAGTGAATTT | 57117 |
| rs758050419 | in-del | -/CTTCT | | | upstream-variant-2KB, intron-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105709386 | CTTGGGTCACACTAA[-/CTTCT]CTTCTCTCTTTGGCA | 57117 |
| rs758098416 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105706572 | CCATGTTTCCAAATG[C/T]TTAGTGTATGTGTCT | 57117 |
| rs758289565 | snp | C/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105694170 | CTGGTTAATCATTCC[C/G]CTATGATAAATCAGT | 57117 |
| rs758305634 | snp | A/C | 1.65468e-05 | 0.00287631 | intron-variant | INTS12 | GRCh38.p7 | 4:105692179 | CTACTTTTTTAAATG[A/C]CATAATTTAAAGTTA | 57117 |
| rs758385125 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105703505 | CAGCTCACATTCTGT[A/G]GTCCACCCTTTCAAT | 57117 |
| rs758483910 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105700259 | CATATCGATGGTAAC[A/G]TTTTAAATCCAGGTA | 57117 |
| rs758621387 | snp | A/G | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant, downstream-variant-500B | INTS12, ARHGEF38 | GRCh38.p7 | 4:105683034 | AAGGTTAGAGGTGGA[A/G]GTGGTTTTAAAGGTA | 57117 |
| rs758626537 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105694801 | AAAATCTTAATTACT[A/G]TATGTAGAAATCATC | 57117 |
| rs758640342 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105690206 | TGAAGCAGTGAGAGA[A/G]AGGGCTGTAAGGTAG | 57117 |
| rs758666032 | snp | C/T | 1.64749e-05 | 0.00287005 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105683127 | GCCAGACCAGTCAAA[C/T]CCACAGGTTTCTGGT | 57117 |
| rs758721415 | snp | A/C | | | intron-variant | INTS12 | GRCh38.p7 | 4:105690759 | GGAGCTAAAGTGATA[A/C]TAATAATGAAACAGT | 57117 |
| rs758824296 | snp | C/T | 1.7886e-05 | 0.00299044 | intron-variant | INTS12 | GRCh38.p7 | 4:105699814 | GTACTACAGGCCTTA[C/T]AAAACTCTCTCCAAG | 57117 |
| rs759097745 | snp | G/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105701491 | TCTACATAATGATAG[G/T]TACAGAAAAATTATT | 57117 |
| rs759142019 | in-del | -/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105684145 | CTTCAACTTCTCTGA[-/T]TAACTTTCCTGGCTA | 57117 |
| rs759152804 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105688743 | GACCCACCTAACTTG[C/T]ATGTTTTAACAGATA | 57117 |
| rs759152820 | snp | A/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105703212 | AGAAAAATGTATATA[A/T]GAAAGATATTTAATA | 57117 |
| rs759195590 | snp | C/T | 4.94173e-05 | 0.00497053 | missense, nc-transcript-variant, downstream-variant-500B | INTS12, ARHGEF38 | GRCh38.p7 | 4:105683014 | GACTAAGGCCAGTTT[C/T]ACCCAAGGTTAGAGG | 57117 |
| rs759294477 | snp | G/T | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | INTS12, GSTCD | GRCh38.p7 | 4:105708801 | TACTTCCCTTTTTCC[G/T]GTCCGCCGGATTATG | 57117 |
| rs759315963 | snp | C/T | 1.66607e-05 | 0.00288619 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105699881 | TAACTGGAATCAATG[C/T]CCCGAGCCAAAGATT | 57117 |
| rs759316232 | snp | A/T | 1.65444e-05 | 0.00287609 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105695667 | TTGGGTGGCTCCACA[A/T]CCTAAAAGATGAAAA | 57117 |
| rs759345748 | snp | C/T | | | upstream-variant-2KB, intron-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105709716 | TCATAAATTCTTGAA[C/T]ATCAAGAAAATGCCA | 57117 |
| rs759525047 | snp | A/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105683372 | TAATCAGTACCTGTA[A/T]AAACATCCCAAGTTA | 57117 |
| rs759652939 | snp | A/C | | | intron-variant | INTS12 | GRCh38.p7 | 4:105698235 | TAAATGAATATCAAC[A/C]AATATTCATGTTAGA | 57117 |
| rs759776922 | snp | C/T | 6.78449e-05 | 0.0058239 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105683308 | AATTTCCTGAAATAA[C/T]TGTGGATGTCTAAAA | 57117 |
| rs759796070 | snp | A/C | | | intron-variant | INTS12 | GRCh38.p7 | 4:105705931 | TGCCTACTGTTGTAA[A/C]CCCTGTCTGGCAGAG | 57117 |
| rs759996806 | snp | C/T | 1.65974e-05 | 0.0028807 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | INTS12, ARHGEF38 | GRCh38.p7 | 4:105682728 | CAAAAACCTACTTGG[C/T]CACATTACTTCTTGA | 57117 |
| rs760048221 | snp | A/G | 1.65198e-05 | 0.00287395 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105693314 | CTACAAACAACGCAG[A/G]CCAATCCCATCTCCA | 57117 |
| rs760142151 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105691379 | GAAAACTATCCAATA[C/T]AACAAATGAAAAGAT | 57117 |
| rs760144974 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105684205 | CTATATAAATACATA[C/T]TGCTCTTGTTCACAC | 57117 |
| rs760157456 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105704306 | GGTTCCTCCTATCCA[A/G]TTAAAAATGAGTTCC | 57117 |
| rs760176872 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105708948 | TCGGACTGGGCGGGA[A/G]GGCGCAGGCGGCCCA | 57117 |
| rs760214760 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105690569 | AAAAAACTGGATAAT[A/G]GAACAACTTTCACTT | 57117 |
| rs760300690 | snp | A/G | 2.07278e-05 | 0.00321923 | intron-variant | INTS12 | GRCh38.p7 | 4:105692138 | CACCATCATTTGCCT[A/G]AGAAAACATACCATT | 57117 |
| rs760317339 | in-del | -/TATAAACATCCCAAGT | | | intron-variant | INTS12 | GRCh38.p7 | 4:105683370 | TTTAATCAGTACCTG[-/TATAAACATCCCAAGT]TATGAATTGGGAAAT | 57117 |
| rs760473279 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105686469 | ATTTTGGAATGATCA[C/T]AGACTGTTCGTATTT | 57117 |
| rs760490132 | snp | A/C | | | intron-variant | INTS12 | GRCh38.p7 | 4:105698327 | AAAGTTTGAGAAACA[A/C]TGGCATAAATCACTC | 57117 |
| rs760536359 | snp | A/G | 1.64822e-05 | 0.00287068 | synonymous-codon, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105683194 | GTGTTGTTGAACTCA[A/G]TTTTGCTGTTGAAGG | 57117 |
| rs760583218 | snp | A/G | 0.00010393 | 0.00720794 | intron-variant | INTS12 | GRCh38.p7 | 4:105700020 | TTGCAAACGCCTGAA[A/G]GAAAAAAAGAGAAAG | 57117 |
| rs760589249 | snp | A/G | 6.58979e-05 | 0.00573974 | synonymous-codon, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105683102 | ACCTATTCCACCTTT[A/G]GATGATGTTGCCAGA | 57117 |
| rs760708236 | snp | A/C | 1.65509e-05 | 0.00287666 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105699891 | CAATGCCCCGAGCCA[A/C]AGATTCATCAAGCAG | 57117 |
| rs760748122 | snp | A/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105684445 | TATAATTTAGAACTT[A/T]ACTCTGAAATAGTTG | 57117 |
| rs760825483 | snp | G/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105699496 | CCTTTTACTTGATTT[G/T]TTTTAATCCTTAAAA | 57117 |
| rs760827084 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105706135 | ATTGTCCAAGTATTT[A/G]TCCTTGGCTATCTTC | 57117 |
| rs761008669 | snp | G/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105700568 | AAACTCACCTCTTCA[G/T]TTCTCTGCCCCAACC | 57117 |
| rs761046582 | snp | A/G | 3.30382e-05 | 0.00406423 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105686792 | GCTGGAGTTACAGAA[A/G]CAACTGCAGGGGCTG | 57117 |
| rs761155176 | snp | A/C | | | intron-variant | INTS12 | GRCh38.p7 | 4:105691333 | TGAAATTCATTTATC[A/C]TTTATCTATTTTATA | 57117 |
| rs761181547 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105693750 | CTTTGTACTCTTCTA[C/T]CTACTAAAGAATTAT | 57117 |
| rs761212476 | snp | G/T | 1.64781e-05 | 0.00287033 | missense, nc-transcript-variant, downstream-variant-500B | INTS12, ARHGEF38 | GRCh38.p7 | 4:105682876 | TAGTTTTGCTGGTAG[G/T]ACTTCCACTAGGTCC | 57117 |
| rs761246787 | snp | A/G | 3.29462e-05 | 0.00405857 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | INTS12, ARHGEF38 | GRCh38.p7 | 4:105682988 | GCTGACATTGTCACA[A/G]CTAACTGAGCGACTA | 57117 |
| rs761469707 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105691541 | AGACAGATATGCACA[C/T]ATAAATATCGCCTCT | 57117 |
| rs761479582 | snp | C/G | 1.64768e-05 | 0.00287021 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105693350 | AAATCATCAGCACTG[C/G]TCTCCTCAAAACTGG | 57117 |
| rs761574598 | in-del | -/TTTTT/TTTTTTT | | | upstream-variant-2KB, intron-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105710232 | TAGTGGGCCCATCAA[-/TTTTT/TTTTTTT]TTTTTTTTTTTTTTT | 57117 |
| rs761653811 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105699684 | CTATGTGGTGTAACA[A/G]TTCTCTGAAAACTTG | 57117 |
| rs761661250 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105689563 | TCCCCATTTAGTACT[C/T]TGACTTCTGGACACA | 57117 |
| rs761745759 | in-del | -/GC | | | intron-variant | INTS12 | GRCh38.p7 | 4:105701176 | GTCCCCTCCCCTCCA[-/GC]TTCACTCCTCATCCT | 57117 |
| rs761972211 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105688246 | GGGAAAGATGCTTCC[C/T]GCCAGCCATTCCATA | 57117 |
| rs762016772 | snp | C/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | INTS12, GSTCD | GRCh38.p7 | 4:105708544 | GAGGAGCGAGGAAAC[C/T]AATACCCCACGTAGC | 57117 |
| rs762031787 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105697789 | GTGTGGTGACACATG[C/T]CTGTAATCCCAGCAC | 57117 |
| rs762253571 | snp | A/G | 1.89838e-05 | 0.00308083 | synonymous-codon, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105692066 | CTGGGGTTTATGACA[A/G]TCTCGGTGGTAGAGA | 57117 |
| rs762286632 | snp | A/C | | | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105683115 | TTGGATGATGTTGCC[A/C]GACCAGTCAAACCCA | 57117 |
| rs762306662 | snp | C/T | 6.45161e-05 | 0.00567925 | intron-variant | INTS12 | GRCh38.p7 | 4:105691947 | AACATTGACAGACTG[C/T]TTAAAATAAAGAAAA | 57117 |
| rs762393921 | snp | A/G | | | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105699864 | CCTTTTGAGATGGAC[A/G]GTAACTGGAATCAAT | 57117 |
| rs762497667 | snp | A/T | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant, downstream-variant-500B | INTS12, ARHGEF38 | GRCh38.p7 | 4:105683004 | CTAACTGAGCGACTA[A/T]GGCCAGTTTTACCCA | 57117 |
| rs762623676 | snp | C/T | 4.94303e-05 | 0.00497119 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | INTS12, ARHGEF38 | GRCh38.p7 | 4:105682889 | AGTACTTCCACTAGG[C/T]CCTGATGTTCCACTA | 57117 |
| rs762633389 | snp | A/C | | | intron-variant | INTS12 | GRCh38.p7 | 4:105691146 | TACTTCTGACCTTTA[A/C]AAGATATATTGGTTA | 57117 |
| rs762699595 | snp | C/T | 1.64787e-05 | 0.00287038 | synonymous-codon, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105695618 | TGATATTTTGGGCTC[C/T]TGCTTAATGGAAATG | 57117 |
| rs762729152 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105687717 | GGGAGGCTGAGGCGG[A/G]TGGTTCACTTGAGGT | 57117 |
| rs762734895 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105686943 | GAAATACAGTTGAAC[A/G]TTTTAAAAAATAGTG | 57117 |
| rs762734917 | snp | C/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105705717 | GTAGAAAGTGTGCCA[C/G]CCCCACCTCCATCTT | 57117 |
| rs762787177 | in-del | -/AGAT | | | intron-variant | INTS12 | GRCh38.p7 | 4:105690793 | GTACATACTAAAGAA[-/AGAT]AGATTATTGTCACAA | 57117 |
| rs762795772 | snp | G/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105688534 | ATATTAAGAATGTTC[G/T]AAGTAATTCACTGTT | 57117 |
| rs762867968 | snp | A/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | INTS12, GSTCD | GRCh38.p7 | 4:105708478 | TCCTCACTGAAAGGG[A/G]AGAGCAGTCAGTCTA | 57117 |
| rs762981236 | snp | A/G | 0.000215666 | 0.010382 | synonymous-codon, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105683254 | CTGCCCATCCAGTTA[A/G]GCCACTAGTTACTGA | 57117 |
| rs763074455 | snp | C/T | 1.93812e-05 | 0.00311291 | synonymous-codon, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105683300 | ACTAGAAGAATTTCC[C/T]GAAATAACTGTGGAT | 57117 |
| rs763103493 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105696012 | GTGCACCACCACACC[C/T]GGCTGATTTTTGTAG | 57117 |
| rs763186556 | snp | A/C | 1.76101e-05 | 0.00296728 | intron-variant | INTS12 | GRCh38.p7 | 4:105700037 | AAAAAAAGAGAAAGT[A/C]ATCTAGAAGACAATG | 57117 |
| rs763338508 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105704226 | CATGAGTCATTCGCC[A/G]CCTCAGTCAGGTAAA | 57117 |
| rs763427077 | in-del | -/TT | 3.30442e-05 | 0.0040646 | frameshift-variant, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105699931 | CTTTTCAGCAGAATC[-/TT]TACTCTTTGAATGCA | 57117 |
| rs763485349 | snp | C/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105697260 | ACTTTGGCAGCTCTT[C/G]GAATTCCCCCTCCCC | 57117 |
| rs763585404 | snp | G/T | 5.71434e-05 | 0.00534495 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105692083 | CTCGGTGGTAGAGAT[G/T]ATGGCACTCCTGACA | 57117 |
| rs763615024 | snp | A/G | 3.31318e-05 | 0.00406999 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | INTS12, ARHGEF38 | GRCh38.p7 | 4:105682730 | AAAACCTACTTGGCC[A/G]CATTACTTCTTGAGT | 57117 |
| rs763668022 | snp | A/T | 1.65026e-05 | 0.00287246 | synonymous-codon, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105693319 | AACAACGCAGGCCAA[A/T]CCCATCTCCATGGCA | 57117 |
| rs763841149 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105691193 | AATTCATTTGATTAA[C/T]AGACATGAGAACTCT | 57117 |
| rs764089589 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105706387 | AGCCTCCCAAGCAGC[C/T]AGGACTACAGGCATG | 57117 |
| rs764127467 | snp | C/T | 1.64757e-05 | 0.00287012 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105683113 | CTTTGGATGATGTTG[C/T]CAGACCAGTCAAACC | 57117 |
| rs764178746 | snp | C/G | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant, downstream-variant-500B | INTS12, ARHGEF38 | GRCh38.p7 | 4:105683026 | TTTTACCCAAGGTTA[C/G]AGGTGGAGGTGGTTT | 57117 |
| rs764298936 | snp | C/G | 1.66638e-05 | 0.00288645 | intron-variant | INTS12 | GRCh38.p7 | 4:105695692 | TGAAAAAAGGTACCA[C/G]TAATTAAATATTTAG | 57117 |
| rs764467188 | snp | A/G | 3.30803e-05 | 0.00406682 | intron-variant | INTS12 | GRCh38.p7 | 4:105691942 | ACAAAAACATTGACA[A/G]ACTGTTTAAAATAAA | 57117 |
| rs764508490 | snp | A/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105693867 | TAAGATATAAATATT[A/T]TCAATATACCCATTA | 57117 |
| rs764697662 | snp | A/C | | | intron-variant, upstream-variant-2KB | INTS12, GSTCD | GRCh38.p7 | 4:105707380 | GTACTTTAAGGGCAG[A/C]GTCTATATTTATCTT | 57117 |
| rs764737730 | snp | A/G | 1.64773e-05 | 0.00287026 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | INTS12, ARHGEF38 | GRCh38.p7 | 4:105682886 | GGTAGTACTTCCACT[A/G]GGTCCTGATGTTCCA | 57117 |
| rs764868914 | snp | A/C | 1.71487e-05 | 0.00292815 | intron-variant | INTS12 | GRCh38.p7 | 4:105695475 | CTGCTTATGGAACAA[A/C]TAATTTACTTTCTTT | 57117 |
| rs764900429 | snp | A/G | 1.66037e-05 | 0.00288125 | synonymous-codon, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105686827 | CTGCGGTGGTTTCTG[A/G]GTTTTTTGAGCCTGC | 57117 |
| rs764914077 | snp | C/T | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105693371 | TCAAAACTGGAAAGG[C/T]CAGCCATAGGTAAAT | 57117 |
| rs765135990 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105699794 | GTCTATATGTTATCA[A/G]TGTAGTACTACAGGC | 57117 |
| rs765146467 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105701224 | GAAACACACATACAC[A/G]TCCCTAGGCTTTTTT | 57117 |
| rs765178952 | snp | A/G | 1.65712e-05 | 0.00287843 | synonymous-codon, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105683249 | AAAAGCTGCCCATCC[A/G]GTTAAGCCACTAGTT | 57117 |
| rs765207219 | snp | A/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105684819 | TAAAACTGTCTGCCA[A/T]ATGGTTAAATGATCT | 57117 |
| rs765214532 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105698658 | CATATTGATTTGGTC[A/G]ATCTGAACTCACTGA | 57117 |
| rs765359541 | snp | C/T | 3.29489e-05 | 0.00405874 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105683119 | ATGATGTTGCCAGAC[C/T]AGTCAAACCCACAGG | 57117 |
| rs765486460 | snp | C/G | 3.3066e-05 | 0.00406595 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105699945 | CTTTACTCTTTGAAT[C/G]CAAGAAACCTAGTGC | 57117 |
| rs765546356 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105706520 | TTCCCAAAGTGCTGG[A/G]ATTACAAGTGCGAGC | 57117 |
| rs765597873 | snp | A/C | | | intron-variant, upstream-variant-2KB | INTS12, GSTCD | GRCh38.p7 | 4:105707517 | TTGTAGCCATTTCCA[A/C]GGTCCCTTCAGCAAA | 57117 |
| rs765833604 | snp | A/T | 3.13465e-05 | 0.00395882 | intron-variant | INTS12 | GRCh38.p7 | 4:105691953 | GACAGACTGTTTAAA[A/T]TAAAGAAAAATATGA | 57117 |
| rs765984885 | snp | A/G | 1.64727e-05 | 0.00286986 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | INTS12, ARHGEF38 | GRCh38.p7 | 4:105683006 | AACTGAGCGACTAAG[A/G]CCAGTTTTACCCAAG | 57117 |
| rs766031414 | snp | A/G | | | intron-variant, downstream-variant-500B, nc-transcript-variant | INTS12, ARHGEF38 | GRCh38.p7 | 4:105682342 | ACCCAGAATACGGGG[A/G]GGAAAATAGAAAACT | 57117 |
| rs766039357 | snp | C/T | 4.95585e-05 | 0.00497763 | synonymous-codon, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105695660 | TGAAATTTTGGGTGG[C/T]TCCACATCCTAAAAG | 57117 |
| rs766201842 | snp | A/T | 3.40936e-05 | 0.00412864 | intron-variant | INTS12 | GRCh38.p7 | 4:105695486 | ACAACTAATTTACTT[A/T]CTTTTAACAAGATTA | 57117 |
| rs766225765 | in-del | -/ATC | | | intron-variant | INTS12 | GRCh38.p7 | 4:105700691 | TCTCTGAGGGATAAT[-/ATC]ATATCTACTTAAAAC | 57117 |
| rs766276383 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105688570 | CTTGATTACTGGTAC[C/T]AGCAGGAAAGCAGAG | 57117 |
| rs766336404 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105686980 | TAATGAATATATATG[C/T]TCTTTGACAAATTAT | 57117 |
| rs766382427 | snp | C/T | 4.18104e-05 | 0.00457203 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105683305 | AAGAATTTCCTGAAA[C/T]AACTGTGGATGTCTA | 57117 |
| rs766417529 | snp | G/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105701373 | AGGCCAGTACTATAA[G/T]GAAAAAGTAACCTTA | 57117 |
| rs766481373 | in-del | -/GCTTG | 1.74449e-05 | 0.00295332 | intron-variant | INTS12 | GRCh38.p7 | 4:105700028 | CCTGAAGGAAAAAAA[-/GCTTG]GAGAAAGTAATCTAG | 57117 |
| rs766618674 | snp | C/T | 1.66131e-05 | 0.00288206 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105683257 | CCCATCCAGTTAAGC[C/T]ACTAGTTACTGACGA | 57117 |
| rs766674045 | in-del | -/C | | | intron-variant | INTS12 | GRCh38.p7 | 4:105704659 | ATATCATTGGTGCCT[-/C]CTATGCAACGTGTCT | 57117 |
| rs766679010 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105690797 | ATACTAAAGAAAGAT[A/G]GATTATTGTCACAAT | 57117 |
| rs766680941 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105704293 | AGTCATCTTTGTAGG[C/T]TCCTCCTATCCAATT | 57117 |
| rs766712985 | in-del | -/TG | | | intron-variant | INTS12 | GRCh38.p7 | 4:105703180 | TAGAAAACAAAGTCC[-/TG]TGTGTGTGTGTATGA | 57117 |
| rs766726689 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105693721 | AGAACAGTTTAACAA[A/G]TATTTGTATTTCTCT | 57117 |
| rs766773400 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105691334 | GAAATTCATTTATCA[C/T]TTATCTATTTTATAA | 57117 |
| rs766863487 | snp | A/G | 1.68499e-05 | 0.00290253 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | INTS12, ARHGEF38 | GRCh38.p7 | 4:105682712 | TTAGGCTAATATGAT[A/G]CAAAAACCTACTTGG | 57117 |
| rs766959813 | snp | C/G | 1.96003e-05 | 0.00313046 | synonymous-codon, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105692114 | TTCTACTAATTGATT[C/G]CCAGATGCCACCATC | 57117 |
| rs767090070 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105688779 | TAATTATGATGAAGC[C/T]CCAGGAAGTACTTCT | 57117 |
| rs767137181 | snp | C/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105690388 | GAGATTTATTAAGTG[C/G]CTATTGCAATAGACA | 57117 |
| rs767168985 | snp | C/T | 1.64757e-05 | 0.00287012 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105683080 | TGTTATTGGAACCTA[C/T]TTTGGAACCTATTCC | 57117 |
| rs767239041 | snp | A/G | | | upstream-variant-2KB, intron-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105709760 | ATTGTGTGCTACATT[A/G]TTGATAAAGAAGGTG | 57117 |
| rs767268215 | snp | C/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105700083 | TAAAGTTTTACTTTT[C/G]TGTTTTTTAATTTGT | 57117 |
| rs767350124 | snp | C/G | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant, downstream-variant-500B | INTS12, ARHGEF38 | GRCh38.p7 | 4:105683016 | CTAAGGCCAGTTTTA[C/G]CCAAGGTTAGAGGTG | 57117 |
| rs767471813 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105708817 | GTCCGCCGGATTATG[A/G]ATGACGGCCGGCGCG | 57117 |
| rs767514862 | in-del | -/AC | | | intron-variant | INTS12 | GRCh38.p7 | 4:105700707 | TCATATCTACTTAAA[-/AC]ACACACACACACACA | 57117 |
| rs767603232 | snp | C/T | 1.64988e-05 | 0.00287213 | synonymous-codon, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105695531 | TTTATCAGCAGGTCT[C/T]TTTTCAGCTTCCTTC | 57117 |
| rs767725260 | snp | G/T | 1.64982e-05 | 0.00287208 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105686770 | CTTAACCAATGGATC[G/T]TTGACAGCTGGAGTT | 57117 |
| rs767776705 | snp | C/T | 2.25864e-05 | 0.00336046 | synonymous-codon, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105683309 | ATTTCCTGAAATAAC[C/T]GTGGATGTCTAAAAA | 57117 |
| rs767899127 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105704456 | ATTCCTAGGCCTACT[A/G]AAGAAAAAACTCTGG | 57117 |
| rs767999081 | snp | A/G | 1.68012e-05 | 0.00289833 | intron-variant | INTS12 | GRCh38.p7 | 4:105693528 | ATAAAGTAATGTGGT[A/G]GAATAAACTTTAAGT | 57117 |
| rs768009103 | snp | C/T | 1.82377e-05 | 0.00301969 | intron-variant | INTS12 | GRCh38.p7 | 4:105700058 | GAAGACAATGCACAA[C/T]TATCTATGTTAAAGT | 57117 |
| rs768053027 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105691795 | GAAAAATGCACATAA[C/T]ATGGTCTGGTCTTTA | 57117 |
| rs768107133 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105705959 | GAGTTCCTGGAAAAC[A/G]GCAAATAACTGTAAA | 57117 |
| rs768392389 | in-del | -/A | | | intron-variant | INTS12 | GRCh38.p7 | 4:105700755 | CACACAGAGCCTATG[-/A]TGCTTTGTGTCCTAA | 57117 |
| rs768398965 | snp | A/T | 5.39593e-05 | 0.00519391 | intron-variant | INTS12 | GRCh38.p7 | 4:105686664 | AACTTTAAGATATAA[A/T]CTTAGATAAAAATAG | 57117 |
| rs768401673 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105704122 | TTCTCAGAAATCATA[C/T]GCTTTTGTACTCTTT | 57117 |
| rs768441442 | snp | A/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105699501 | TACTTGATTTTTTTT[A/T]ATCCTTAAAATATTA | 57117 |
| rs768527201 | snp | G/T | 1.72472e-05 | 0.00293654 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105683281 | CTGACGAGGAAACGC[G/T]GGCACTAGAAGAATT | 57117 |
| rs768691106 | snp | A/C | | | intron-variant | INTS12 | GRCh38.p7 | 4:105687978 | ACAACAGAAAAAAAA[A/C]CAGCAACTATTTTTC | 57117 |
| rs768697883 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105694277 | AAAGCACATAGTTGA[A/G]TGGAGAAAAAGTTAC | 57117 |
| rs768706883 | snp | A/G | 1.73996e-05 | 0.00294949 | intron-variant | INTS12 | GRCh38.p7 | 4:105700022 | GCAAACGCCTGAAGG[A/G]AAAAAAGAGAAAGTA | 57117 |
| rs768714170 | snp | A/G | 1.71082e-05 | 0.00292469 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | INTS12, ARHGEF38 | GRCh38.p7 | 4:105682682 | GATTATATCATAATA[A/G]TAAGCCTTTCATCTT | 57117 |
| rs768753395 | snp | C/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105685825 | GTAGTATGATTTCAA[C/G]GATGCAAACTTAGGA | 57117 |
| rs768836780 | snp | C/T | 1.71997e-05 | 0.0029325 | intron-variant | INTS12 | GRCh38.p7 | 4:105693259 | GGGTCATGTGTTCTT[C/T]ATAAAGTAACAAAAG | 57117 |
| rs768922381 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105700461 | TGTGTAAGGGCTATC[A/G]TAAGAGGGCAATGGT | 57117 |
| rs768933032 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105683440 | TCTTATGAAGCTGAT[C/T]TGAAAAACCACACAG | 57117 |
| rs769076212 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105696936 | TTTAATTTAAATTTC[C/T]CCAGTAACTAATGAT | 57117 |
| rs769103752 | snp | A/C | | | upstream-variant-2KB, intron-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105709273 | CCCTAGCCAGTCCCT[A/C]ATGTCTTCCTCTGCT | 57117 |
| rs769128380 | snp | A/C/T | 3.29501e-05 | 0.00405884 | synonymous-codon, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105683057 | TAAAGGTACAGTGGG[A/C/T]GTAGTGCTGTTATTG | 57117 |
| rs769255360 | snp | A/G | 3.54032e-05 | 0.00420718 | intron-variant | INTS12 | GRCh38.p7 | 4:105699829 | CAAAACTCTCTCCAA[A/G]CTTTTTATTCATTCA | 57117 |
| rs769255405 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105694419 | TAACCTCCGCCTGCT[A/G]GGTTAGAGTGATTCT | 57117 |
| rs769269364 | in-del | -/TC | | | intron-variant | INTS12 | GRCh38.p7 | 4:105689612 | GATTTCTGGTACTAA[-/TC]TGCATTTAGCCTGGC | 57117 |
| rs769393586 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105691023 | TTGATATACACACTT[C/T]TCATTTACTACTTTT | 57117 |
| rs769483033 | snp | C/T | | | intron-variant, utr-variant-5-prime | INTS12 | GRCh38.p7 | 4:105702910 | CCCTTTTCTGTTGCC[C/T]TCTCTAATCTCTGTT | 57117 |
| rs769534430 | snp | A/G | 1.68153e-05 | 0.00289955 | intron-variant | INTS12 | GRCh38.p7 | 4:105686688 | AAAATAGAATCTACT[A/G]TACCTTGACTTCTGT | 57117 |
| rs769636280 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105688435 | CCTTAAATCTCAATT[C/T]GTATCACTTTTTATA | 57117 |
| rs769807375 | snp | A/G | 1.68221e-05 | 0.00290014 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105683271 | CCACTAGTTACTGAC[A/G]AGGAAACGCTGGCAC | 57117 |
| rs769868282 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105692992 | AGCAATCACCATAGC[C/T]TTAGATTATCAAAGG | 57117 |
| rs769883106 | snp | C/T | 1.70394e-05 | 0.0029188 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | INTS12, ARHGEF38 | GRCh38.p7 | 4:105682698 | TAAGCCTTTCATCTT[C/T]AGGCTAATATGATAC | 57117 |
| rs769921395 | snp | C/T | | | upstream-variant-2KB, intron-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105709399 | AACTTCTCTTCTCTC[C/T]TTGGCATTGAGTTTT | 57117 |
| rs769947222 | snp | C/T | | | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | INTS12, GSTCD | GRCh38.p7 | 4:105708664 | GCCCTGCCGATCCGT[C/T]TGTTCCCGGTGGTCC | 57117 |
| rs770214214 | in-del | -/AAAAAAGGTACCAGTA | 1.65888e-05 | 0.00287996 | intron-variant | INTS12 | GRCh38.p7 | 4:105695679 | ACATCCTAAAAGATG[-/AAAAAAGGTACCAGTA]ATTAAATATTTAGAC | 57117 |
| rs770242765 | snp | C/T | 1.69677e-05 | 0.00291266 | intron-variant | INTS12 | GRCh38.p7 | 4:105693278 | AAGTAACAAAAGAAT[C/T]TGTGGCAAGGTACAA | 57117 |
| rs770244437 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105698130 | TGCAGTATTAAACTA[C/T]TACCTAATTCAGCAA | 57117 |
| rs770297724 | snp | A/C | | | intron-variant | INTS12 | GRCh38.p7 | 4:105683874 | AAAAAAAAATGTCCT[A/C]CTAAATTTTGAGCAA | 57117 |
| rs770307049 | snp | C/T | 1.64757e-05 | 0.00287012 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105683166 | GAAGTAGCAGGTTTC[C/T]CAGTATTGTTTTGTG | 57117 |
| rs770360239 | snp | C/T | 3.40078e-05 | 0.00412344 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105700005 | TCACAGTAGCAGCCA[C/T]TGCAAACGCCTGAAG | 57117 |
| rs770439025 | in-del | -/ATC | | | intron-variant, upstream-variant-2KB | INTS12, GSTCD | GRCh38.p7 | 4:105707069 | ACTGGCACAAAAATT[-/ATC]ATTCATCATCCCCAG | 57117 |
| rs770443214 | snp | G/T | 1.64749e-05 | 0.00287005 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105683059 | AAGGTACAGTGGGCG[G/T]AGTGCTGTTATTGGA | 57117 |
| rs770612172 | snp | C/T | 6.79844e-05 | 0.00582989 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105699863 | ACCTTTTGAGATGGA[C/T]GGTAACTGGAATCAA | 57117 |
| rs770648219 | snp | G/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105691274 | GGGAGAGGTGGAGAA[G/T]AAGACATTATGGCAA | 57117 |
| rs770724268 | snp | C/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105690162 | ACTTAGTCTGTGTCA[C/G]AGTGGCCAGAGTGTA | 57117 |
| rs770760811 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105690525 | AAGAGGCATCAAAGA[C/T]GTTTTCTAATTCAGG | 57117 |
| rs770812993 | snp | C/T | | | intron-variant, utr-variant-5-prime, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105703705 | CAACTTGGCAATTCT[C/T]TCATCCTTCTCTGGT | 57117 |
| rs771049735 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105698191 | TAAGTTTTAACTCCA[C/T]TATTTCACATTTGCC | 57117 |
| rs771095056 | snp | G/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | INTS12, GSTCD | GRCh38.p7 | 4:105708039 | ATGGCTCTAAAAAAC[G/T]TTGTTCTTCATGACT | 57117 |
| rs771097835 | snp | C/G | | | upstream-variant-2KB, intron-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105709700 | AGGATCCCATTCCTT[C/G]TCATAAATTCTTGAA | 57117 |
| rs771256651 | snp | G/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105705033 | TCTCACAATCCAAAG[G/T]TTCAAGAATAAGATT | 57117 |
| rs771258551 | snp | C/T | 1.64741e-05 | 0.00286998 | missense, nc-transcript-variant, downstream-variant-500B | INTS12, ARHGEF38 | GRCh38.p7 | 4:105682950 | CCTGGAACTAAACTA[C/T]TTGGACTAGGAAGAC | 57117 |
| rs771383244 | snp | A/T | 3.29478e-05 | 0.00405867 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | INTS12, ARHGEF38 | GRCh38.p7 | 4:105682832 | TGGGCCTTTAAGGGA[A/T]GCTGAGGGAGAGCTG | 57117 |
| rs771402540 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105699105 | GTAGTTCTTATTATC[C/T]CCATTTTACCAATAA | 57117 |
| rs771484245 | snp | C/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105704089 | CATCTTCTATCTTTT[C/G]TCTTTTATAGCAAAA | 57117 |
| rs771738779 | in-del | -/GGTTTCTCCAATCTA | 1.64732e-05 | 0.0028699 | cds-indel, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105693428 | GATGACTGTGTTTCT[-/GGTTTCTCCAATCTA]GGTTTCTTTGGAATA | 57117 |
| rs771744344 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105698749 | ACAATAAAAAGGCTT[C/T]GGAGTACTAGACCTA | 57117 |
| rs771892675 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105686343 | ATCCACCCGCCTTGG[C/T]CTCCCAAAGTGCTGG | 57117 |
| rs771941321 | snp | C/T | 3.44335e-05 | 0.00414916 | utr-variant-5-prime, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105700014 | CAGCCATTGCAAACG[C/T]CTGAAGGAAAAAAAG | 57117 |
| rs771984432 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105683780 | AGAACATATCCAAGA[C/T]GAAGAGATTCAGTCA | 57117 |
| rs772103293 | snp | A/G | 1.89532e-05 | 0.00307835 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105692023 | AATACCACACCAGGC[A/G]AGGGTCATTCGCTTC | 57117 |
| rs772156246 | snp | C/T | 6.77897e-05 | 0.00582153 | intron-variant | INTS12 | GRCh38.p7 | 4:105691928 | GAAAGCACATACCAA[C/T]AAAAACATTGACAGA | 57117 |
| rs772192367 | snp | C/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105691339 | TCATTTATCATTTAT[C/G]TATTTTATAAGTGAA | 57117 |
| rs772333892 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105698265 | AATACACTTGGAGAC[C/T]TGGTAATGTTAGTAA | 57117 |
| rs772430446 | snp | C/T | 1.64754e-05 | 0.00287009 | missense, nc-transcript-variant, downstream-variant-500B | INTS12, ARHGEF38 | GRCh38.p7 | 4:105682864 | TGGATTCTGAAGTAG[C/T]TTTGCTGGTAGTACT | 57117 |
| rs772470403 | in-del | -/TTA | | | intron-variant | INTS12 | GRCh38.p7 | 4:105697680 | TTACTATTTGGCTCT[-/TTA]TTATAAAGTCTGTTG | 57117 |
| rs772485782 | snp | C/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | INTS12, GSTCD | GRCh38.p7 | 4:105708278 | ATCACACATCGAAGT[C/G]CTAGAATGGGGGATG | 57117 |
| rs772517536 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105687744 | AGGTCAGGAGTTTGC[A/G]AACAGCCAGAACAGC | 57117 |
| rs772541193 | snp | A/G | 3.29451e-05 | 0.00405851 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | INTS12, ARHGEF38 | GRCh38.p7 | 4:105682979 | ACCTACTTTGCTGAC[A/G]TTGTCACAACTAACT | 57117 |
| rs772604596 | snp | C/G | 1.64781e-05 | 0.00287033 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105695574 | GTTGTGAGGACCTTG[C/G]CATTATTATTACCAG | 57117 |
| rs772729618 | snp | C/T | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant, downstream-variant-500B | INTS12, ARHGEF38 | GRCh38.p7 | 4:105683002 | AACTAACTGAGCGAC[C/T]AAGGCCAGTTTTACC | 57117 |
| rs772786860 | snp | A/C | 3.29565e-05 | 0.00405921 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105695615 | GGATGATATTTTGGG[A/C]TCTTGCTTAATGGAA | 57117 |
| rs772876889 | snp | C/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105694440 | GAGTGATTCTCACGT[C/G]TCAGCCTCCTGAGGT | 57117 |
| rs772948558 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105688477 | CCACATCAAAGTACA[C/T]CTACCTTCAACATCA | 57117 |
| rs773038113 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105701169 | TTTTGTTGTCCCCTC[C/T]CCTCCAGCTTCACTC | 57117 |
| rs773082181 | in-del | -/TAGAT | | | intron-variant | INTS12 | GRCh38.p7 | 4:105695244 | AGGATCTCTGAGGCA[-/TAGAT]TAAAGTTTACACTCA | 57117 |
| rs773089195 | snp | C/G | 5.67746e-05 | 0.00532767 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105683298 | GCACTAGAAGAATTT[C/G]CTGAAATAACTGTGG | 57117 |
| rs773222296 | snp | A/G | | | upstream-variant-2KB, intron-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105709498 | ACTTGCTTCATTTGG[A/G]GCCATTTGCTTATGT | 57117 |
| rs773441486 | in-del | -/ATTC | 1.76306e-05 | 0.00296901 | intron-variant | INTS12 | GRCh38.p7 | 4:105699836 | CTCTCCAAGCTTTTT[-/ATTC]ATTCAAGTACCTTTT | 57117 |
| rs773446957 | snp | C/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105702822 | CAGAAAACAGTAGTT[C/G]AACCTAAAATAAAAC | 57117 |
| rs773462382 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105689778 | AGGCCTGGTGGCACA[C/T]GCCTGTAGTCCCAGC | 57117 |
| rs773645421 | snp | C/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105683999 | AATTTGCCCATGATT[C/G]CGGTTAAACTATCAT | 57117 |
| rs773690168 | snp | G/T | 3.37678e-05 | 0.00410886 | intron-variant | INTS12 | GRCh38.p7 | 4:105693282 | AACAAAAGAATCTGT[G/T]GCAAGGTACAACTTA | 57117 |
| rs773788321 | snp | A/G | 3.81236e-05 | 0.00436581 | synonymous-codon, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105692078 | ACAATCTCGGTGGTA[A/G]AGATTATGGCACTCC | 57117 |
| rs773809344 | snp | A/G | 1.64746e-05 | 0.00287002 | synonymous-codon, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105683063 | TACAGTGGGCGTAGT[A/G]CTGTTATTGGAACCT | 57117 |
| rs773880335 | snp | A/T | | | synonymous-codon, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105683264 | AGTTAAGCCACTAGT[A/T]ACTGACGAGGAAACG | 57117 |
| rs773932066 | snp | C/T | 1.68001e-05 | 0.00289823 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105699870 | GAGATGGACGGTAAC[C/T]GGAATCAATGCCCCG | 57117 |
| rs774099023 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105693623 | TAGTTAGGGACAGAT[A/G]TGCACATTAAAGATC | 57117 |
| rs774174531 | snp | A/T | 1.65198e-05 | 0.00287395 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105695661 | GAAATTTTGGGTGGC[A/T]CCACATCCTAAAAGA | 57117 |
| rs774224571 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105691297 | TATGGCAATTTCTTG[C/T]TTTCTTTAAAAGAAA | 57117 |
| rs774394296 | snp | C/T | 1.65135e-05 | 0.00287341 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105686736 | AAGTTGTCTCTTGTT[C/T]CAGTTTAGTTTCTGG | 57117 |
| rs774454777 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105690227 | TGTAAGGTAGAGTCG[A/G]GTCAAAAAGAGAAGG | 57117 |
| rs774590713 | snp | A/G | | | upstream-variant-2KB, intron-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105709703 | ATCCCATTCCTTGTC[A/G]TAAATTCTTGAATAT | 57117 |
| rs774640615 | snp | C/T | | | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105683317 | AAATAACTGTGGATG[C/T]CTAAAAAAATAAAGT | 57117 |
| rs774648087 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105697070 | TATTACTAAGTTAAA[A/G]GAGTTCTTCATAGAT | 57117 |
| rs774652292 | snp | A/G | 1.66671e-05 | 0.00288674 | intron-variant | INTS12 | GRCh38.p7 | 4:105693507 | AAAAGCAGGCATCAG[A/G]AAATGATAAAGTAAT | 57117 |
| rs774881809 | snp | A/G | 1.64738e-05 | 0.00286995 | missense, nc-transcript-variant, downstream-variant-500B | INTS12, ARHGEF38 | GRCh38.p7 | 4:105682833 | GGGCCTTTAAGGGAT[A/G]CTGAGGGAGAGCTGC | 57117 |
| rs774933016 | snp | A/C | 6.69299e-05 | 0.0057845 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | INTS12, ARHGEF38 | GRCh38.p7 | 4:105682719 | AATATGATACAAAAA[A/C]CTACTTGGCCACATT | 57117 |
| rs775014569 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105703336 | CCTAGGGAAGTGGTA[A/G]TAGTAGTATTGATAG | 57117 |
| rs775130220 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105704105 | TCTTTTATAGCAAAA[C/T]GTTCTCAGAAATCAT | 57117 |
| rs775335467 | snp | G/T | 1.64751e-05 | 0.00287007 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105683092 | CTATTTTGGAACCTA[G/T]TCCACCTTTGGATGA | 57117 |
| rs775362129 | snp | C/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105686437 | TATCTAACCAGATGA[C/G]AATGGTAAAGAATGT | 57117 |
| rs775371974 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105705605 | TTGACACTCATTAAA[C/T]GTTACCTAGTATCTT | 57117 |
| rs775399743 | snp | A/C | 1.73105e-05 | 0.00294193 | intron-variant | INTS12 | GRCh38.p7 | 4:105700019 | ATTGCAAACGCCTGA[A/C]GGAAAAAAAGAGAAA | 57117 |
| rs775542578 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105691362 | TAAGTGAATAAAAGT[C/T]AGAAAACTATCCAAT | 57117 |
| rs775708555 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105699446 | TCTCTTAAATTATCC[C/T]ACCCATATTCAATTT | 57117 |
| rs775799521 | snp | C/T | 4.94173e-05 | 0.00497053 | missense, nc-transcript-variant, downstream-variant-500B | INTS12, ARHGEF38 | GRCh38.p7 | 4:105682980 | CCTACTTTGCTGACA[C/T]TGTCACAACTAACTG | 57117 |
| rs775801291 | snp | A/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105684436 | ATATCCAGTTATAAT[A/T]TAGAACTTTACTCTG | 57117 |
| rs775818000 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105705978 | AATAACTGTAAATGT[C/T]GGCCAAGTAAATACT | 57117 |
| rs775857972 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105699148 | AAATGAAGTTTCTAT[A/G]TACCTCAGTTTCCTT | 57117 |
| rs775993485 | snp | C/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105694471 | GCTGGAACTACAGGT[C/G]TGCGCCACCACACCT | 57117 |
| rs776000219 | in-del | -/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105687227 | TCTTCTTGGGGTCTA[-/G]GGCATAAGTCGACTC | 57117 |
| rs776026638 | in-del | -/TA | | | intron-variant | INTS12 | GRCh38.p7 | 4:105690276 | TGAGTATAATCTCAT[-/TA]TATAAGTAATTGAGA | 57117 |
| rs776047943 | snp | C/T | 1.64784e-05 | 0.00287035 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105695577 | GTGAGGACCTTGCCA[C/T]TATTATTACCAGAAG | 57117 |
| rs776092945 | snp | A/C | 1.68474e-05 | 0.00290231 | intron-variant | INTS12 | GRCh38.p7 | 4:105693530 | AAAGTAATGTGGTAG[A/C]ATAAACTTTAAGTCA | 57117 |
| rs776128246 | snp | A/T | 1.64773e-05 | 0.00287026 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | INTS12, ARHGEF38 | GRCh38.p7 | 4:105682874 | AGTAGTTTTGCTGGT[A/T]GTACTTCCACTAGGT | 57117 |
| rs776138720 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105693131 | ACAATTTTCAATATG[C/T]TAAATTGTTATATGG | 57117 |
| rs776167835 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105691427 | AAGGCAGGTATGTTA[A/G]TCAACAGTAAAAAGA | 57117 |
| rs776355021 | snp | A/C | | | intron-variant | INTS12 | GRCh38.p7 | 4:105699553 | GTGGTTACATTCAGC[A/C]GCTTAAAAAAAATTC | 57117 |
| rs776495050 | snp | A/T | 1.73999e-05 | 0.00294952 | intron-variant | INTS12 | GRCh38.p7 | 4:105700024 | AAACGCCTGAAGGAA[A/T]AAAAGAGAAAGTAAT | 57117 |
| rs776562212 | snp | A/C | | | intron-variant | INTS12 | GRCh38.p7 | 4:105703233 | ATATTTAATATATTA[A/C]ATGTAGGTTTCATTT | 57117 |
| rs776586918 | snp | A/G | 1.82377e-05 | 0.00301969 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105683292 | ACGCTGGCACTAGAA[A/G]AATTTCCTGAAATAA | 57117 |
| rs776639783 | snp | A/G | 1.64912e-05 | 0.00287147 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105683208 | AATTTTGCTGTTGAA[A/G]GACCAGCAGAGGAAG | 57117 |
| rs776811934 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105686618 | GTTTCTCATTAAATT[C/T]TTTATCAAGCAACTA | 57117 |
| rs776835823 | snp | A/G | 3.25166e-05 | 0.00403203 | intron-variant | INTS12 | GRCh38.p7 | 4:105691946 | AAACATTGACAGACT[A/G]TTTAAAATAAAGAAA | 57117 |
| rs776911725 | snp | C/T | | | intron-variant, upstream-variant-2KB | INTS12, GSTCD | GRCh38.p7 | 4:105707417 | TATCTCTTTGCCACT[C/T]TGCAAAGTACAACAA | 57117 |
| rs777067025 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105696977 | TTTTCAAGTGTTCAT[A/G]TGGCATACATATATC | 57117 |
| rs777226269 | in-del | -/T | 1.64732e-05 | 0.0028699 | frameshift-variant, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105693430 | TGACTGTGTTTCTGG[-/T]TTCTCCAATCTAGGT | 57117 |
| rs777249029 | snp | C/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | INTS12, GSTCD | GRCh38.p7 | 4:105708525 | GTAAATTATGATTCC[C/T]CTTGAGGAGCGAGGA | 57117 |
| rs777288650 | snp | C/T | 1.76902e-05 | 0.00297402 | intron-variant | INTS12 | GRCh38.p7 | 4:105699830 | AAAACTCTCTCCAAG[C/T]TTTTTATTCATTCAA | 57117 |
| rs777297165 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105701687 | ACTAATCTTTCTACT[A/G]ATTTTATTTCATATA | 57117 |
| rs777436485 | in-del | -/AGC | 1.64751e-05 | 0.00287007 | cds-indel, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105683156 | GTTAGCTGACGAAGT[-/AGC]AGGTTTCCCAGTATT | 57117 |
| rs777452141 | snp | A/G | 5.00104e-05 | 0.00500027 | intron-variant | INTS12 | GRCh38.p7 | 4:105686851 | AGCCTGCAAAAATCA[A/G]TGGATTAAATCAGAT | 57117 |
| rs777522465 | snp | A/G | 4.20195e-05 | 0.00458344 | synonymous-codon, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105691994 | TCTTTTCATTTGTCT[A/G]GTACATCGGGCACAA | 57117 |
| rs777678431 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105696443 | TGCATTTCCTAGAAA[C/T]TTATATAAATGGAAT | 57117 |
| rs777729920 | snp | A/G | | | downstream-variant-500B | INTS12, ARHGEF38 | GRCh38.p7 | 4:105682551 | TAGAATAAAAATGTT[A/G]AAGATTGATTTAAAA | 57117 |
| rs777838609 | snp | C/T | | | intron-variant, utr-variant-5-prime, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105703654 | TATACATACATTCTA[C/T]CTTCAGAATCACCAT | 57117 |
| rs777943422 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | INTS12, ARHGEF38 | GRCh38.p7 | 4:105682692 | TAATAATAAGCCTTT[C/T]ATCTTTAGGCTAATA | 57117 |
| rs778081826 | snp | A/C/T | 3.29664e-05 | 0.00405984 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105695551 | CAGCTTCCTTCTTTA[A/C/T]CTTTTCAGTTGTGAG | 57117 |
| rs778085922 | snp | C/T | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant, downstream-variant-500B | INTS12, ARHGEF38 | GRCh38.p7 | 4:105682816 | GTGATTCTTGTGAAG[C/T]TGGGCCTTTAAGGGA | 57117 |
| rs778175826 | snp | C/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105704607 | CTCTGCAGTCCATGT[C/G]TCTCTCCCAAGATCC | 57117 |
| rs778201231 | in-del | -/CAAAGTACAA | | | intron-variant, upstream-variant-2KB | INTS12, GSTCD | GRCh38.p7 | 4:105707420 | CTCTTTGCCACTTTG[-/CAAAGTACAA]CAAAATAATGGCTAT | 57117 |
| rs778225895 | snp | A/C | | | intron-variant | INTS12 | GRCh38.p7 | 4:105697829 | CCAAGGTGGGCAGAT[A/C]ACTTGAGTCCAGGAG | 57117 |
| rs778332849 | snp | A/C | 3.66482e-05 | 0.00428051 | intron-variant | INTS12 | GRCh38.p7 | 4:105683328 | GATGTCTAAAAAAAT[A/C]AAGTAAATAATTACA | 57117 |
| rs778333714 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | INTS12, ARHGEF38 | GRCh38.p7 | 4:105682708 | ATCTTTAGGCTAATA[C/T]GATACAAAAACCTAC | 57117 |
| rs778608759 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105709015 | CGCGCCTCTGCGACC[A/G]GGTAAAGAGGGCGCT | 57117 |
| rs778655853 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105696620 | CCTATTGATGGATAT[C/T]TGGGTTGTCTGCAGT | 57117 |
| rs778674232 | in-del | -/TACCTACA | 0.000100098 | 0.00707384 | intron-variant | INTS12 | GRCh38.p7 | 4:105693295 | TGGCAAGGTACAACT[-/TACCTACA]TACCTACAAACAACG | 57117 |
| rs778714209 | snp | C/G | 6.82571e-05 | 0.00584156 | | | GRCh38.p7 | 4:105692164 | CCATTAAACATTACA[C/G]TACTTTTTTAAATGC | 57117 |
| rs778767204 | snp | C/T | 2.01924e-05 | 0.00317739 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105692001 | ATTTGTCTGGTACAT[C/T]GGGCACAATACCACA | 57117 |
| rs778986287 | snp | A/G | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant, downstream-variant-500B | INTS12, ARHGEF38 | GRCh38.p7 | 4:105683031 | CCCAAGGTTAGAGGT[A/G]GAGGTGGTTTTAAAG | 57117 |
| rs779020194 | snp | C/T | | | intron-variant, utr-variant-5-prime, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105703730 | TCTGGTCAACTCACT[C/T]CCCCACTTTCTGCAA | 57117 |
| rs779086456 | snp | G/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105687641 | AGAGTCAAACACAGT[G/T]AGGATTAAAACCCAG | 57117 |
| rs779315833 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105700139 | TAAAATTTAAAATCA[C/T]CAAAAAGTTATTACA | 57117 |
| rs779316195 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105694070 | ACTATTAACATGACA[C/T]ATGTATAAAGTAGCT | 57117 |
| rs779322467 | snp | C/T | 1.64735e-05 | 0.00286993 | missense, nc-transcript-variant, downstream-variant-500B | INTS12, ARHGEF38 | GRCh38.p7 | 4:105682951 | CTGGAACTAAACTAC[C/T]TGGACTAGGAAGACC | 57117 |
| rs779353865 | snp | A/C | 3.29625e-05 | 0.00405958 | synonymous-codon, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105695558 | CTTCTTTACCTTTTC[A/C]GTTGTGAGGACCTTG | 57117 |
| rs779363833 | snp | C/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105704341 | TGCTAGGTTCTGGGT[C/G]TCTTCTTGACTTGTT | 57117 |
| rs779564137 | in-del | -/C | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | INTS12, GSTCD | GRCh38.p7 | 4:105708788 | TAGGAAGTGACGTTA[-/C]TTCCCTTTTTCCGGT | 57117 |
| rs779738992 | snp | A/C | 1.74717e-05 | 0.00295559 | intron-variant | INTS12 | GRCh38.p7 | 4:105683361 | AGAGCCAAGTTTAAT[A/C]AGTACCTGTATAAAC | 57117 |
| rs779794617 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105683746 | AATAGCAAAAATGCC[C/T]ATACCCAGAATATTC | 57117 |
| rs779826195 | snp | A/C | 1.64754e-05 | 0.00287009 | missense, nc-transcript-variant, downstream-variant-500B | INTS12, ARHGEF38 | GRCh38.p7 | 4:105682787 | CATCTGTAATCGCTT[A/C]ATAGCATTGAGCTGT | 57117 |
| rs779836035 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105704946 | AAAAGCTTAATCAGT[C/T]TCCCACAATCACTCT | 57117 |
| rs779839014 | snp | C/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105697985 | AACCTGGGAGGGAGA[C/G]AGCGCAGTGAGCCAA | 57117 |
| rs779839943 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105694219 | TATTATGTAGTAGCT[A/G]AAAGAAATCTAGATC | 57117 |
| rs779840192 | snp | A/G | 0.000115313 | 0.0075923 | synonymous-codon, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105693438 | TTTCTGGTTTCTCCA[A/G]TCTAGGTTTCTTTGG | 57117 |
| rs780015914 | snp | C/T | 1.87876e-05 | 0.00306488 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105692040 | GGGTCATTCGCTTCC[C/T]TGTCTGTCACCTGGG | 57117 |
| rs780076546 | snp | A/T | 3.15941e-05 | 0.00397442 | intron-variant | INTS12 | GRCh38.p7 | 4:105692184 | TTTTTAAATGCCATA[A/T]TTTAAAGTTATTTCA | 57117 |
| rs780133669 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105694818 | ATGTAGAAATCATCT[A/G]AAAATAGACAATCCA | 57117 |
| rs780186895 | snp | C/T | 4.94246e-05 | 0.0049709 | synonymous-codon, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105683150 | TTTCTGGTTAGCTGA[C/T]GAAGTAGCAGGTTTC | 57117 |
| rs780206193 | in-del | -/A | | | intron-variant | INTS12 | GRCh38.p7 | 4:105701675 | CTGTGACAGTTTACT[-/A]ATCTTTCTACTGATT | 57117 |
| rs780402638 | in-del | -/ATC | | | intron-variant | INTS12 | GRCh38.p7 | 4:105689477 | TTAGGCTCACTTCAG[-/ATC]ATGTCTTTTGGTATT | 57117 |
| rs780484939 | snp | C/G | 1.78245e-05 | 0.00298529 | intron-variant | INTS12 | GRCh38.p7 | 4:105699823 | GCCTTACAAAACTCT[C/G]TCCAAGCTTTTTATT | 57117 |
| rs780496601 | snp | A/G | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant, downstream-variant-500B | INTS12, ARHGEF38 | GRCh38.p7 | 4:105683037 | GTTAGAGGTGGAGGT[A/G]GTTTTAAAGGTACAG | 57117 |
| rs780746779 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105706709 | AACTTTCTTTTAGTC[A/G]GGTTTGAGACCAAAG | 57117 |
| rs780978864 | snp | A/G | 1.64738e-05 | 0.00286995 | stop-gained, nc-transcript-variant, downstream-variant-500B | INTS12, ARHGEF38 | GRCh38.p7 | 4:105682924 | CATTCCCACTTAGTT[A/G]GCTGCTGCTTCCTGG | 57117 |
| rs780980004 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105685546 | TTTTTAAAAGTATTT[C/T]GTATTCATATTCTTT | 57117 |
| rs780985386 | snp | A/C | | | intron-variant | INTS12 | GRCh38.p7 | 4:105695422 | ATACCTATACCCATT[A/C]TTATATAAAAGAAAT | 57117 |
| rs781029500 | snp | C/G | 1.71413e-05 | 0.00292752 | intron-variant | INTS12 | GRCh38.p7 | 4:105686679 | TCTTAGATAAAAATA[C/G]AATCTACTATACCTT | 57117 |
| rs781035623 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105687148 | AAACTATATGTAACC[A/G]TTAGCTTTACTCATG | 57117 |
| rs781084081 | snp | A/T | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | INTS12, GSTCD | GRCh38.p7 | 4:105707924 | TTCACCCTACCTGGC[A/T]ATCTCAAAAGAAGTC | 57117 |
| rs781182838 | snp | A/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105689543 | GTTATAATATTAGCC[A/G]TGACTCCCCATTTAG | 57117 |
| rs781212211 | snp | C/T | 1.71944e-05 | 0.00293205 | intron-variant | INTS12 | GRCh38.p7 | 4:105693261 | GTCATGTGTTCTTTA[C/T]AAAGTAACAAAAGAA | 57117 |
| rs781267812 | snp | A/C | | | intron-variant | INTS12 | GRCh38.p7 | 4:105703557 | ACCCGAAAGCCCTGT[A/C]GTTTCCCTACTTTAT | 57117 |
| rs781363003 | snp | C/G | 1.64751e-05 | 0.00287007 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105693443 | GGTTTCTCCAATCTA[C/G]GTTTCTTTGGAATAT | 57117 |
| rs781587837 | in-del | -/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105704758 | AAATGATATTTACCC[-/T]ATTGCCCAAGCCAGT | 57117 |
| rs781590777 | snp | C/G | 3.37804e-05 | 0.00410963 | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105699998 | TCCAAGTTCACAGTA[C/G]CAGCCATTGCAAACG | 57117 |
| rs781636304 | snp | C/G | | | upstream-variant-2KB, intron-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105710678 | CCATTTAGATTAAAA[C/G]AAGCACAGGTATTGT | 57117 |
| rs781757287 | snp | A/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105685209 | CTTTTATAAAAAGTG[A/T]ATTTTTTATTAAAGA | 57117 |
| rs781770502 | snp | C/T | | | upstream-variant-2KB, intron-variant | GSTCD, INTS12 | GRCh38.p7 | 4:105709370 | TGTTACTTCAAGACC[C/T]CTTGGGTCACACTAA | 57117 |
| rs796081043 | snp | C/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105705639 | CCATTCTCACTCTCT[C/G]TGTTATAGCTATCTG | 57117 |
| rs796323884 | snp | A/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105700735 | CACACACACACACAC[A/T]CACACACACAGAGCC | 57117 |
| rs796365876 | snp | C/G | | | intron-variant | INTS12 | GRCh38.p7 | 4:105697798 | CACATGCCTGTAATC[C/G]CAGCACTTTGGGAAG | 57117 |
| rs796566881 | snp | C/T | | | intron-variant | INTS12 | GRCh38.p7 | 4:105691369 | ATAAAAGTTAGAAAA[C/T]TATCCAATATAACAA | 57117 |
| rs796806990 | snp | C/G | | | missense, nc-transcript-variant | INTS12 | GRCh38.p7 | 4:105693362 | CTGGTCTCCTCAAAA[C/G]TGGAAAGGTCAGCCA | 57117 |